Search Results - Longmuir, Susannah

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  1. 1
    Practical community photoscreening in very young children

    Practical community photoscreening in very young children by Longmuir, Susannah Q, Boese, Erin A, Pfeifer, Wanda, Zimmerman, Bridget, Short, Lori, Scott, William E

    Published in Pediatrics (Evanston)
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  2. 2
    A family with branchio-oculo-facial syndrome with primarily ocular involvement associated with mutation of the TFAP2A gene

    A family with branchio-oculo-facial syndrome with primarily ocular involvement associated with mutation of the TFAP2A gene by Dumitrescu, Alina V., Milunsky, Jeff M., Longmuir, Susannah Q., Drack, Arlene V.

    Published in Ophthalmic genetics
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  3. 3
    A novel 4p16.3 microduplication distal to WHSC1 and WHSC2 characterized by oligonucleotide array with new phenotypic features

    A novel 4p16.3 microduplication distal to WHSC1 and WHSC2 characterized by oligonucleotide array with new phenotypic features by Cyr, Andrew B., Nimmakayalu, Manjunath, Longmuir, Susannah Q., Patil, Shivanand R., Keppler‐Noreuil, Kim M., Shchelochkov, Oleg A.

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  4. 4
    Use of a Supplemental Oxygen Protocol to Suppress Progression of Retinopathy of Prematurity

    Use of a Supplemental Oxygen Protocol to Suppress Progression of Retinopathy of Prematurity by Colaizy, Tarah T, Longmuir, Susannah, Gertsch, Kevin, Abràmoff, Michael David, Klein, Jonathan M

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  5. 5
    Neurodevelopmental outcome of preterm infants enrolled in myo-inositol randomized controlled trial

    Neurodevelopmental outcome of preterm infants enrolled in myo-inositol randomized controlled trial by Adams-Chapman, Ira, Watterberg, Kristi L., Nolen, Tracy L., Hirsch, Shawn, Cole, Carol A., Cotten, C. Michael, Oh, William, Poindexter, Brenda B., Zaterka-Baxter, Kristin M., Das, Abhik, Lacy, Conra Backstrom, Scorsone, Ann Marie, Duncan, Andrea F., DeMauro, Sara B., Goldstein, Ricki F., Colaizy, Tarah T., Wilson-Costello, Deanne E., Purdy, Isabell B., Hintz, Susan R., Heyne, Roy J., Myers, Gary J., Fuller, Janell, Merhar, Stephanie, Harmon, Heidi M., Peralta-Carcelen, Myriam, Kilbride, Howard W., Maitre, Nathalie L., Vohr, Betty R., Natarajan, Girija, Mintz-Hittner, Helen, Quinn, Graham E., Wallace, David K., Olson, Richard J., Orge, Faruk H., Tsui, Irena, Gaynon, Michael, Hutchinson, Amy K., He, Yu-Guang, Winter, Timothy W., Yang, Michael B., Haider, Kathryn M., Cogen, Martin S., Hug, Denise, Bremer, Don L., Donahue, John P., Lucas, William R., Phelps, Dale L., Higgins, Rosemary D.

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  6. 6
    A family with branchio-oculo-facial syndrome with primarily ocular involvement associated with mutation of the TFAP2A gene

    A family with branchio-oculo-facial syndrome with primarily ocular involvement associated with mutation of the TFAP2A gene by Dumitrescu, Alina V., Milunsky, Jeff M., Longmuir, Susannah Q., Drack, Arlene V.

    Published in Ophthalmic Genetics
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  7. 7
    A novel 4p16.3 microduplication distal to WHSC1 and WHSC2 characterized by oligonucleotide array with new phenotypic features

    A novel 4p16.3 microduplication distal to WHSC1 and WHSC2 characterized by oligonucleotide array with new phenotypic features by Cyr, Andrew B., Nimmakayalu, Manjunath, Longmuir, Susannah Q., Patil, Shivanand R., Keppler-Noreuil, Kim M., Shchelochkov, Oleg A.

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